Pilot Study of Bone Mineral Density Changes During Anti-PD-1 Immunotherapy

Recruiting N/A Interventional Study
Breast Cancer (Triple Negative Breast Cancer (TNBC)) Renal Cell Carcinoma (Kidney Cancer) Melanoma (Skin Cancer) Non-Small Cell Lung Cancer MSI-H/dMMR Rectal Cancer Squamous Cell Carcinoma Mouth Invasive Mammary Carcinoma Classic Hodgkin Lymphoma
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
25 (estimated)
Sponsor
Jessica Mezzanotte Sharpe · Other
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About This Trial
Immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment and work by blocking protein interactions that normally prevent the immune system from recognizing and destroying cancer cells. However, these agents, now approved for over 15 types of cancers and for both early-stage and metastatic disease, are capable of causing inflammation in any organ system of the body that can lead to …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Age ≥ 18 years. 2. Patients planning to start or within the first four weeks of treatment with anti-PD-1 immune checkpoint inhibitor therapy either alone or in combination with chemotherapy for curative intent for a known cancer diagnosis (use of immunotherapy must be FDA-app…
Contacts

Jessica Sharpe, MD, PhD

615-936-8422

jessica.m.sharpe@vumc.org

CONTACT